Human Genetics 1993: Vol 91 Table of Contents

7 Pages·1993·0.36 MB·English

III
Contents of Volume 91
Bardoni B, Floridia G, Guioli S, Peverali gene for the tricyclic antidepressant-
Abbreviations in parenthesis refer to G, Anichini C, Cistemino M, Casalone sensitive noradrenaline transporter (SC)
the following sections: (E) Editorial;
R, Danesino C, Fraccaro M, Zuffardi O, 278
(R) Review article; (O) Original inves¬
Camerino G: Functional disomy of Brun P Poulat F
tigation; (SC) Short communication; Xp22-pter in three males carrying a por¬ Bureau J-F —> Lefebvre S
(CC) Clinical case report; (CO) Case tion of Xp translocated to Yq (O) 333 Buys CHCM Kooy RF
observed; (RG) Rare genetic variant Barsky SH Grody WW Byrne JA, Smith PJ: The 1 lpl5.5 ribonu¬
register; (DV) DNA variants; (L) Letter Barth ML, Fensom A, Harris A: Preva¬ cleotide reductase M1 subunit locus is
to the editors; (ER) Erratum
lence of common mutations in the aryl- not imprinted in Wilms’ tumour and he¬
sulphatase A gene in metachromatic patoblastoma (SC) 275
leukodystrophy patients diagnosed in
Britain (SC) 73 Caligaris-Cappio F —> Ghia P
Ahmad M —> Faiyaz ul Haque M Bartholome K —* Liidecke B Calugi A —» De Vita R
Ainsworth PJ, Rodenhiser DI, Costa MT: Batista DAS —> Tuck-Muller CM Camerino G —> Bardoni B
Identification and characterization of Baudi F Marasco O Cannizzaro LA, Aronson MM, Thiesen
sporadic and inherited mutations in exon Bayliss JD —» Shoulders CC HJ: Human zinc finger gene ZNF23
31 of the neurofibromatosis (NFl) gene Beck JS, Kwitek AE, Cogen PH, Metzger (Koxl6) maps to a zinc finger gene clus¬
(O) 151 AK, Duyk GM, Sheffield VC: A dena¬ ter on chromosome 16q22, and ZNF32
Aksentijevich 1. Gruberg L, Pras E, Balow turing gradient gel electrophoresis assay (Kox30) to chromosome region
JE Jr, Kovo M, Gazit E, Dean M, Pras for sensitive detection of p53 mutations 10q23-q24(SC) 383
M, Kastner DL: Evidence for linkage of (O) 25 Cans C, Cohen O, Mermet M-A, Demon-
the gene causing familial Mediterranean Beersum SEC van —> Mariman ECM geot J, Jalbert P: Human reciprocal
fever to chromosome 17q in non-Ash¬ Beigel Y -4 Leitersdorf E translocations: is the unbalanced mode
kenazi Jewish families: second locus or Benmammar D —> De Juan D at birth predictable? (O) 228
type 1 error? (O) 527 Berriche S —> Lucotte G Caporossi D Tedeschi B
Alembik Y -> Stoll C Berta P —> Poulat F Caridi G —> Ghiggeri GM
Almeida A. Kokalj-Vokac N, Lefrancois Bignell P —4 Millar DS Casalone R —> Bardoni B
D, Viegas-Pequignot E, Jeanpierre M, Bird TD ^ Lebo RV Casals T, Nunes V, Palacio A, Gimenez J,
Dutrillaux B, Malfoy B: Hypomethyla- Blakemore AIF —» Tarlow JK Gaona A, Ibanez N, Mortal N, Estivill
tion of classical satellite DNA and chro¬ Blaschak J —> Warren AC X: Cystic fibrosis in Spain: high fre¬
mosome instability in lymphoblastoid Blayau M -4 Dorval I quency of mutation G542X in the
cell lines (O) 538 Bodvarsson M —> Fossdal R Mediterranean coastal area (O) 66
Alterman LA —¥ O’Reilly M-AJ Bonisch H —> Briiss M Cavallo D ^ De Vita R
Altieri P —> Ghiggeri GM Boileau C —» Saint-Jore B Cederbaum SD Grody WW
Andersen T1 —» Lindblom A Bonaiti-Pellie C, Chompret A, Toumade Chakravarti A —> Warren AC
Anderson LA Lebo RV M-F, Lemerle J, Voute PA, Delemarre Chance PF Lebo RV
Angotti E —> Marasco O JFM: Excess of multifocal tumors in Chauvel B —4 Dorval 1
Anichini C —> Bardoni B nephroblastoma: implications for mecha¬ Chenevix-Trench G, Healey S, Martin NG:
Antonarakis SE —> Warren AC nisms of tumor development and genetic Reproductive hormone genes in mothers
Arinami T —» Hamada H counseling (O) 373 of spontaneous dizygotic twins: an asso¬
Armstrong M, Idle JR, Daly AK: A poly¬ Boogaard M-JH van den —> Bouwens- ciation study (O) 118
morphic Cfol site in exon 6 of the hu¬ Rombouts AGM Chompret A —» Bonaiti-Pellie C
man cytochrome P450 CYP2D6 gene Boomsma DI Knijff P de Chroniary K —> Tzimagiorgis G
detected by the polymerase chain reac¬ Boscherini B —> Tedeschi B Cianfarani S -4 Tedeschi B
tion (DV) 616 Bottema CDK, Ketterling RP, Vielhaber E, Cistemino M —» Bardoni B
Amaiz-Villena A —> De Juan D Yoon H-S, Gostout B, Jacobson DP, Clarke A Upadhyaya M
Aronson MM —» Cannizzaro LA Shapiro A, Sommer SS: The pattern of Claussen U -4 Eggeling F von
Asmundsson P Fossdal R spontaneous germ-line mutation: relative Clegg JB Flint J
Assum G, Fink T, SteinbeiBer T, Fisel KJ: rates of mutation at or near CpG dinu¬ Clegg JB -4 Martinson JJ
Analysis of human extrachromosomal cleotides in the factor IX gene (O) 4% Coetzee GA -4 Leitersdorf E
DNA elements originating from different Bouwens-Rombouts AGM, Boogaard Cogen PH —» Beck JS
^-satellite subfamilies (O) 489 M-JH van den, Puig JG, Mateos FA, Cohen D —> Schachter F
Auburger G —> Lunkes A Hennekam RCM, Tilanus MGJ: Identifi¬ Cohen O —> Cans C
Audrezet MP Guillermit H cation of two new nucleotide mutations Colombi M —» Shipman R
Avvedimento VE —» Marasco O (HPRTuttechi and HPRTMadnd) in exon 3 Colonna A —> Marasco O
of the human hypoxanthine-guanine Conneally PM -4 Lebo RV
Baars FM van —» Mariman ECM phosphoribosyltransferase (HPRT) gene Connor JM —> Norton B
Bahnak BR Vidaud D (O) 451 Cooper DN -4 Millar DS
Bailly S, Giovine FS di. Duff GW: Poly¬ Boyce AJ —> Flint J Corden D —> Millar DS
morphic tandem repeat region in inter¬ Boyce AJ —> Martinson JJ Corell A —> De Juan D
leukin- 1 a intron 6 (DV) 85 Boyd E -4 Murphy MT Costa J-M ^ Vidaud D
Baligadoo S —> Ramasawmy R Bradley LD —> O’Reilly M-AJ Costa MT —» Ainsworth PJ
Balow JE Jr —> Aksentijevich 1 Brahic M —> Lefebvre S Costanzo F -4 Marasco O
Bandyopadhyay AR: A parental combina¬ Brett DJ —> Shoulders CC Courtay C -4 Morris C
tion analysis for ABO-FIP interaction in Breuning MH —> Fossdal R Cox TK —» Warren AC
a Bengali population (O) 377 Briiss M, Kunz J, Lingen B, Bonisch H: Creau-Goldberg N —> Crete N
Baranov VS —> Ivaschenko TE Chromosomal mapping of the human Cremers CWRJ —> Mariman ECM
IV
Cremers FPM —» Traupe H Drews D -♦ Reiss J protein B-100 in Israeli patients with
Cr6te N. Delabar J-M, Rahmani Z. Yaspo Druck T —» Huebner K dominantly inherited hypercholes¬
M-L. Kraus J, Marks A, Sinet P-M. Duff GW ^ Bailly S terolemia and in offspring with parental
Cr^au-Goldberg N: Partial physical map DuffGW -♦Tarlow JK history of myocardial infarction (L)
of human chromosome 21 from fibro¬ Dumas R —> Poulat F 299
blast and lymphocyte DNA (O) 245 Dutrillaux B Almeida A Fryns JP, Kleczkowska A, Moerman P,
Croce CM —* Huebner K Duyk GM -» Beck JS Vandenberghe K: Hereditary hy¬
Crolla JA —* Wilkinson TA Dyck PJ ^ Lebo RV dronephrosis and the short arm of chro¬
Crossen PE. Morrison MJ: Elevated fre¬ mosome 6 (L) 514
quency of an ETS-1 restriction fragment Eggeling F von. Freytag M. Fahsold R. Fuhrmann W —> Reiss J
polymorphism in chronic B-cell Horsthemke B. Claussen U: Rapid de¬ Fujii H —> Hirono A
leukaemia (SC) 380 tection of trisomy 21 by quantitative Fujiwara Y —» Nakamura M
Cunniff C —» Sawyer JR PCR (O) 567 Fukushima Y, Hoovers J, Mannens M,
Eleuteri P —» De Vita R Wakui K. Ohashi H, Ohno T, Ueoka Y,
Dabadie A —* Dors al I Elion J —» Perichon B Niikawa N: Detection of a cryptic para¬
Dalgleisb R —* Mackay K Ellermeyer U —» Reiss J centric inversion within band 11 pi 3 in
Dallaire A —» De Braekeleer M Enczmann J —* Lunkes A familial aniridia by fluorescence in situ
Daly AK —» Armstrong M Epplen JT —> Niimberg P hybridization (O) 205
Danesino C —* Bardoni B E.stivill X Casals T
Danieli GA, Mioni F. Muller CR. Vitiello Ewenstein BM —* Wise RJ Galindo I —> Premoli-De-Percoco G
L. Mostacciuolo ML. Grimm T: Patterns Ezquieta B, Molano J: CF2603/4delT, a Gaona A —> Casals T
of deletions of the dystrophin gene in new frameshift mutation in exon 13 of Gazengel C —» Vidaud D
different European populations (O) the cystic fibrosis transmembrane con¬ Gazit E —» Aksentijevich I
342 ductance regulator (CFTR) gene (DV) Gendler S —» Lebo RV
Dann EJ —» Friedlander Y 614 Genet SA —> Lovering R
Dann EJ —* Leitersdorf E Gerdes LU —* Hansen PS
David V —» Dorval I Faergeman O —> Hansen PS Gerdes LU Klausen IC
Davies KE —» Rowe PSN Faergeman O —» Klausen IC Gessler M —> Poulat F
Dazin PF —> Lebo RV Fahsold R Eggeling F von Geurts van Kessel A —> Morris C
Dean M —* Aksentijevich I Faiyaz ul Haque M. Uhlhaas S. Knapp M. Gevers Leuven JA —> Knijff P de
Dean M Iva.schenko TE Schiller H. FriedI W, Ahmad M. IYoj>- Ghia P, Dianzani I, Serra A, Rosso C,
De Braekeleer M. Dallaire A. Mathieu J: ping P; Mapping of the gene for X-chro- Caligaris-Cappio F: A frequent £coRI
Genetic epidemiology of sensorimotor mosomal split-hand/split-foot anomaly polymorphism in the bcl-2 gene (DV)
polyneuropathy with or without agenesis toXq26-Kj26.l (O) 17 513
of the corpus callosum in northeastern Famham J —» Upadhyaya M Ghiggeri GM, Caridi G, Altieri P, Pezzolo
(Quebec (O) 223 Fensom A —♦ Barth ML A, Gimelli G, Zuffardi O: Are the nail-
De Juan D, Martin-Villa JM. G6mez- Ferec C —* Guillermit H patella syndrome and the autosomal
Reino JJ. Vicario JL. Corell A. Ferguson-Smith M —» Tzimagiorgis G Goltz-like syndrome the phenotypic ex¬
Martinez-La.so J, Benmammar D. Fey MF. Tobler A: An interleukin-8 (IL-8) pressions of different alleles at the
Amaiz-Villena A: Differential contribu¬ cDNA clone identifies a frequent COL5AI locus?(0) 175
tion of C4 and HLA-DQ genes to sys¬ //i/tdIII polymorphism (DV) 298 Giltay J —» Poulat F
temic lupus erythematosus susceptibility Fink T —» Assum G Gimelli G —» Ghiggeri GM
(O) 579 Fischer HJ —» Schuster H Gimenez J —» Casals T
Delabar J-M —♦ Cr6te N Fisel KJ —» Assum G Giovine FS di —> Bailly S
Delemarre JFM —» Bonaiti-Pelli^ C Fisher LW —♦ Traupe H Gispert S —» Lunkes A
DenKMigeot J —> Cans C Rint J, Harding RM. Clegg JB, Boyce AJ: Gispert-Sanchez S —» Vidaud D
De Vita R. Calugi A. Cavallo D. Eleuteri Why are some genetic diseases com¬ Giuili G, Roechel N, Scholl U, Mattel M-
P, Vizzone A: Flow cytometric and mon? Distinguishing selection from G, Guellaen G: Colocalization of the
cytogenetic analyses in human sponta¬ other processes by molecular analysis of genes coding for the and subunits
neous abortions (O) 409 globin gene variants (R) 91 of soluble guanylyl cyclase to human
Deybach JC ^ Gu X-F Roridia G Bardoni B chromosome 4 at q31.3-q33 (O) 257
Dianzani I —» Ghia P Rye Sainte-Marie F —» Martinson JJ Gotten E —* Zimmer N
Diehl SR ^ Hart TC Focarelli E —» Marasco O Golbus MS —> Lebo RV
Dodson AE —» Grody WW Fossdal R. Bodvarsson M. Asmundsson P, Goldberg EH Miiller U
Domer C —* Steinkasserer A Ragnarsson J, Peters D, Breuning MH. Goldman A -* Hulten M
Dominijanni A —* Marasco O Jensson C): Icelandic families with auto¬ Gomez-Reino JJ —> De Juan D
Donis-Keller H —» Howe JR somal dominant polycystic kidney dis¬ Goossens M —> Vidaud D
Donti E —» Huebner K ease: families unlinked to chromosome Gorlin J —> Wise RJ
Dorval I, Odent S, Jezequel P, Joumel H. I6pl3.3 revealed by linkage analysis Gostout B —> Bottema CDK
Chauvel B, Dabadie A. Roussey M. Le (SC) 609 Goulding J Rowe PSN
Gall JY. Le Marec B. David V, Blayau Fotino L —» Mara.sco O Goulielmos G —» Tzimagiorgis G
M: Analysis of 160 CF chromosomes: Fraccaro M Bardoni B Graadt van Roggen F —» Leitersdorf E
detection of a novel mutation in exon 20 Francomano C —> Petersen GM Grandchamp B —> Gu X-F
(O) 254 Frants RR —» Knijff P de Gregersen N Hansen PS
Dolt B —» Stoll C Frants RR Top B Gregersen N —» Klausen 1C
Dou S Howe JR Fraser RH —> Murphy MT Grimm T —* Danieli GA
Dreesen JCFM. Hurk JAJM van den. Fressinaud E —» Vidaud D Grimm T —> Sander A
Smits APT, Ouweland AMW van den. Freytag M —> Eggeling F von Grody WW, Kern RM, Klein D. Dodson
Markslag PWB. Oost BA van: DXS539, FriedI W —» Faiyaz ul Haque M AE. Wissman PB, Barsky SH, Ceder-
a polymorphic DNA marker proximal of Friedlander Y, Dann EJ, Leitersdorf E: baum SD: Arginase deficiency manifest¬
the fragile-X gene (DV) 80 Absence of familial defective apolipo- ing delayed clinical sequelae and in-
V
duction of a kidney arginase isozyme Hoeve J ten —» Morris C gion of human Xq 12-21.1 using pulsed
(O) 1 Holmes JM, Martin RH: Aneuploidy de¬ field gel electrophoresis (O) 485
Groffen J —> Morris C tection in human sperm nuclei using flu¬ Joumel H —> Dorval 1
Gruberg L —» Aksentijevich I orescence in situ hybridization (O) 20 Junien C —> Saint-Jore B
Grundy CB —» Millar DS Holzknecht RA —* Tsai MY Jury CL Oppenheim A
Gu X-F, Rooij F de, Lee JS, Te Velde K, Hooft FM van’t —» Top B
Deybach JC, Nordmann Y, Grandchamp Hook EB: Choroid plexus cysts diagnosed Kadota Y —> Nakahashi Y
B; High prevalence of a point mutation prenatally as an independent risk factor Ka^ainen H —» Larramendy M
in the porphobilinogen deaminase gene for cytogenetic abnormality (L) 514 Kahkonen M Larramendy M
in Dutch patients with acute intermittent Hoovers J —» Fukushima Y Kajii E, Umenishi F, Iwamoto S, Ikemoto
porphyria (O) 128 Horst J —» Lenz W S: Isolation of a new cDNA clone en¬
Guellaen G —> Giuili G Horsthemke B Eggeling F von coding an Rh polypeptide associated
Guillermit H, Jehanne M, Quere I, Au- Houwen RHJ —> Kooy RF with the Rh blood group system (O)
drezet MP, Mercier B, F6rec C; A novel Howard-Peebles PN —» Plattner R 157
mutation in exon 3 of the CFTR gene Howe JR, Lairmore TC, Veile R, Dou S, Kakimoto Y —> Sano A
(O) 233 Wells SA Jr, Donis-Keller H: Develop¬ Kakkar VV ^ Millar DS
Guioli S —> Bardoni B ment of a sequence-tagged site for the Kalaitsidaki M —> Warren AC
centromere of chromosome 10: its use in Kanno T —> Maekawa M
Hall J ^ Lebo RV cytogenetic and physical mapping (O) Kastner DL —> Aksentijevich I
Hamada H, Arinami T, Kubo T, Hama- 199 Kearns WG —> Tuck-Muller CM
guchi H, Iwasaki H: Fetal nucleated Huebner K, Dmck T, LaForgia S, Lasota J, Keller C —» Schuster H
cells in maternal peripheral bhxxi: fre¬ Croce CM, Lanfrancone L, Donti E, Kempen HJM Knijff P de
quency and relationship to gestational Pengue G, La Mantia G, Pelicci P-G, Kern RM ^ Grody WW
age (O) 427 Lania L: Chromosomal localization of Ketelsen U-P Vries DD de
Hamaguchi H —> Hamada H four human zinc finger cDNAs (O) Ketterling RP Bottema CDK
Hanauer A —» Rowe PSN 217 King MC ^ Lebo RV
Handin Rl ^ Wise RJ Hughes HN ^ Tarlow JK Kinnon C —* Jones AM
Hansen PS, Gerdes LU, Klausen 1C, Hulten M, Goldman A: The relationship Kinnon C —> Lovering R
Gregersen N, Faergeman O; Polymor¬ between meiotic chromosome pairing Kinnon C O’Reilly M-AJ
phisms in the apolipoprotein B-lOO gene and chiasma formation (L) 300 Kintzel D —> Thiel G
contributes to normal variation in plasma Hurk JAJM van den —> Dreesen JCFM Kinzier K Petersen GM
lipids in 464 Danish men bom in 1948 Hurko O —> Lebo RV Kirkwood T Schiichter F
(O) 45 Hyden-Granskog C, Salonen R, Koskull H Kitajima M —> Maekawa M
Hansen PS —> Klausen IC von: Three Finnish incontinentia pig- Kitamura O —> Kubo S
Happle R —> Traupe H menti (IP) families with recombinations Klausen 1C —» Hansen PS
Haraki T —> Inazu A with the IP loci at Xq28 and Xpl I (O) Klausen IC, Hansen PS, Gerdes LU,
Harding RM —» Flint J 185 Rudiger N, Gregersen N, Faergeman O:
Harding RM Martinson JJ A PvmU polymorphism of the low den¬
Harper PS —» Upadhyaya M Ibanez N —> Casals T sity lipoprotein receptor gene is not as¬
Harris A Barth ML Idle JR —> Armstrong M sociated with plasma concentrations of
Hart TC, Marazita ML, McCanna KM, Ikemoto S Kajii E low density lipoproteins including LP(a)
Schenkein HA, Diehl SR: Reevaluation Ikuta T —) Perichon B (SC) 193
of the chromosome 4q candidate region Inazu A, Koizumi J, Haraki T, Yagi K, Kleczkowska A —> Fryns JP
for early onset p)eriodontitis (O) 416 Wakasugi T, Takegoshi T, Mabuchi H, Klein D —> Grody WW
Hassed SJ —» Sawyer JR Takeda R: Rapid detection and preva¬ Knapp M —> Faiyaz ul Haque M
Havekes LM -4 Knijff P de lence of cholesteryl ester transfer protein Knijff P de, Boomsma DI, Wit E de, Kem¬
Havekes LM —> Top B deficiency caused by an intron 14 splic¬ pen HJM, Gevers Leuven JA, Frants
Hay DA —» Loesch DZ ing defect in hyperalphalipoproteinemia RR, Havekes LM: The effect of the
Hayashi N Nakahashi Y (O) 13 apolipoprotein E phenotype on plasma
Hayden M —» Wood S Inoue K —* Nakahashi Y lipids is not influenced by environmental
Healey S —» Chenevix-Trench G Ivaschenko TE, Baranov VS, Dean M: variability: results of a Dutch twin study
Heath JP —» Upadhyaya M Two .iew mutations detected by single¬ (O) 268
Heerema NA —> Plattner R strand conformation polymorphism Knuutila S —> Larramendy M
Heiskanen M —> Larramendy M analysis in cystic fibrosis from Russia Kompf J Krczal D
Heisterkamp N —> Morris C (O) 63 Konig A Poulat F
Henn W —> Zimmer N Iwamoto S Kajii E Koizumi J Inazu A
Hennekam RCM —> Bouwens-Rombouts Iwasaki H —> Hamada H Kokalj-Vokac N —» Almeida A
AGM Kondo I —> Sano A
Himsworth RL Parkinson DB Jacobson DP —> Bottema CDK Kondoh K —> Sano A
Hirono A, Fujii H, Miwa S: Molecular ab¬ Janisch W —> Thiel G Kooy RF, Van der Veen AY, Verlind E,
normality of G6PD Konan and G6PD Jalbert P —> Cans C Houwen RHJ, Scheffer H, Buys CHCM:
Ube, the most common glucose-6-phos- Jarmuz A —> Shoulders CC Physical localisation of the chromosomal
phate dehydrogenase variants in Japan Jaswaney VL —> Muller U marker D13S31 places the Wilson dis¬
(SC) 507 Jeanpierre M —> Almeida A ease locus at the junction of bands ql4.3
Hirose W Kubo S Jehanne M —» Guillermit H and q21.1 of chromosome 13 (SC) 504
Hixson JE, Powers PK, McMahan CA: Jensson 6 —* Fossdal R Koskull H von —> Hyden-Granskog C
The human apolipoprotein B 3' hyper¬ Jesson M —> Wise RJ Koskull H von —» Larramendy M
variable region: detection of eight new Jezequel P —» Dorval I Kotea N Ramasawmy R
alleles and comparisons of allele fre¬ Jiang Z —> Lebo RV Kovo M —> Aksentijevich I
quencies in blacks and whites (O) 475 Jones AM, Malcolm S, Levinsky RJ, Kraus J —» Crete N
Hodges ICG -> Upadhyaya M Kinnon C: Physical mapping in the re¬ Kraus J Zimmer N
VI
Krczal D. Ritter H. Kompf J: Polymor¬ Levinsky RJ —» O’Reilly M-AJ Mannens M —» Fukushima Y
phism of glucose dehydrogenase (GDH. Li SS-L —» Maekawa M Marasco O, Melina F, Mele E, Quaresima
EC 1.1.1.47): formal and population ge¬ Liechti-Gallati S —» Sander A B, Zingone A. Focarelli E, Picciotti E,
netic data (SC) 290 Lindblom A. Skoog L. Andersen TI. Rot- Martelli ML, Fotino L, Vigna MF,
KrishnanHxrrthy R —» Perichon B stein S. Nordenskjold M, Larsson C: Baudi F, Dominijanni A. Angotti E, Pu-
KrishnanHx>rthy R —> Rama.sawmy R Four separate regions on chromosome Jia A, Perrotti N, Colonna A, Mattioli
Kubo S. Kitamurj O. Tsuda R. Hirose W, 17 show loss of heterozygosity in famil¬ PL, Porcellini A, Costanzo F, Avvedi-
Matsumoto H. Nakasono I: Hereditary ial breast carcinomas (O) 6 mento VE: Linkage disequilibrium of
recombined three-allele variant of the Lingen B —» Briiss M three polymorphic RFLP markers in the
Gc system (SC) 71 Loesch DZ, Sheffield LJ, Hay DA: Be- apolipoprotein AI-CIII gene cluster on
Kubo T —> Hamadu H tween-generation differences in ascer¬ chromosome 11 (O) 169
Kuivaniemi H —> Zhuang J tainment and penetrance: relevance to Marazita ML —* Hart TC
Kunz J —» Briiss M genetic hypotheses in fragile X (O) Mariman ECM. Beersum SEC van,
Kwitek AE —» Beck JS 469 Cremers CWRJ, Baars FM van, Ropers
Loux N —» Saint-Jore B HH: Analysis of a second family with
Labie D —* Perichon B Lovelace RE —» Lebo RV hereditary non-chromaffin paragan¬
LaForgia S —* Huebner K Lovering R —¥ O’Reilly M-AJ gliomas locates the underlying gene at
Lairmore TC —* Howe JR Lovering R. Sweatman AK. O’Reilly M- the proximal region of chromosome I Iq
La Mantia G —> Huebner K AJ, Genet SA, Middleton-Price H, Mal¬ (O) 357
Landy SJ —* Traupe H colm S. Levinsky RJ, Kinnon C: Physi¬ Marks A —» Cr6te N
Lanfrancone L —» Huebner K cal mapping identifies DXS265 as a use¬ Markslag PWB —» Dreesen JCFM
Lania L —» Huebner K ful genetic marker for carrier detection Martelli ML —> Mara.sco O
Lanyon WG —* Norton B and prenatal diagnosis of X-linked Martin NG —» Chenevix-Trench G
Lapoumeroulie C —» Perichon B agammaglobulinemia (O) 178 Martin RH Holmes JM
Larramendy M. Heiskanen M. Wessman Lozanova T —* Thiel G Martinez JE —> Tuck-Muller CM
M. Ritvanen A. Peltomaki P. Simola K. Lu C —» Ramasawmy R Martmez-Laso J —> De Juan D
Kaariiiinen H. Koskull H von. Kahkdnen Lucotte G. Berriche S, Turpin JC: A re¬ Martinson JJ, Harding RM. Philippon G,
M. Knuutila S: Molecular cytogenetic combinant Friedreich’s ataxia family Flye Sainte-Marie F, Roux J, Boyce AJ,
study of patients w ith Pallister-Killian (SC) 273 Clegg JB: Demographic reductions and
syndrome (O) 121 Ludwig CU —» Shipman R genetic bottlenecks in humans: min¬
Larsson C —* Lindblom A Ludwig R —* Schneider S isatellite allele distributions in Oceania
La.sota J —» Huebner K Liidecke B, Poller W, Olek K. Bartholome (O) 445
Latov N —» Lebo RV K: Sequence variant of the human Martm-Villa JM —> De Juan D
Lavergne J-M —* Vidaud D cathepsin G gene (DV) 83 Mason JM Osborne LC
Lebo RV. Chance PF, Dyck PJ, Redila- Lund AM —> Mackay K Mateos FA —* Bouwens-Rombouts AGM
Rores MT, Lynch ED, Golbus MS, Bird Lunkes A, Gispert S, Enezmann J, Mathieu J —> De Braekeleer M
TD. King MC. Anderson LA, Hall J, Auburger G: Molecular heterogeneity of Matsumoto H —> Kubo S
Wiegant J, Jiang Z. Dazin PF. Punnett autosomal dominant cerebellar ataxia: Matsuo N —» Ogata T
HH. Schonberg SA. Moore K. Shull analysis of flanking microsatellites of Matsuura Y —» Maekawa M
MM. Gendler S. Hurko O, Lovelace RE. the spinocerebellar ataxia 1 locus in a Mattei M-G —> Giuili G
Latov N, Trofatter J.Conneally PM: northern European family unequivocally Mattei M-G —¥ Lefebvre S
Chromosome I Charcot-Marie-Tooth demonstrates non-linkage (O) 362 Mattioli PL Marasco O
disease (CMTIB) locus in the Fey re¬ Luthman H —¥ Wedell A McCanna KM —» Hart TC
ceptor gene region (ER) 301 Luzzatto L —» Oppenheim A Meinnis MG —» Warren AC
Lee JS ^ Gu X-F Lynch ED —» Lebo RV McMahan CA —> Hixson JE
Lefebvre S, Bureau J-F, Muscatelli F, Meier-Ewert S —» Rowe PSN
Mattei M-G, Brahic M: A new human Ma Y ^ Wood S Meiner V —> Leiteisdorf E
brain cDNA molecule: assignment to Mabuchi H —> Inazu A Mele E —¥ Marasco O
chromosome Ilq2l-q23.1 and descrip¬ Mackay K. Lund AM, Raghunath M. Melina F —> Marasco O
tion of two polymorphisms studied by Steinmann B, Dalgleish R: SSCP Mercier B —> Guillermit H
the polymerase chain reaction (O) 148 detection of a GlyS65Val substitution Mermet M-A —* Cans C
LefraiKois D —* Almeida A in the proal(I) collagen chain resulting Metzger AK —> Beck JS
Le Gall JY ^ Dorval I in osteogenesis imperfecta type II (O) Meyer D —» Vidaud D
Lehrach H Rowe PSN 439 Middleton-Price H Lovering R
Leitersdorf E —* Friedlander Y MacMillan JC —» Upadhyaya M Miles JH Planner R
Leitersdorf E. Reshef A, Meiner V, Dann Maekawa M. Sudo K, Kitajima M, Mat- Miles JS —» Murphy MT
EJ, Beigel Y, Graadt van Roggen F, suura Y, Li SS-L, Kanno T: Analysis of Millar DS, Grundy CB, Bignell P, Mitchell
Westhuyzen DR van der, Coetzee GA: a genetic mutation in an electrophoretic DC. Corden D, Woods P, Kakkar VV,
A missense mutation in the low density variant of the human lactate dehydroge- Cooper DN: A novel nonsense mutation
lipoprotein receptor gene causes familial nase-B(H) subunit (O) 423 in the protein C (PRCXT) gene (Trp-29—>
hypercholesterolemia in Sephardic Jews Maekawa M, Sudo K, Kitajima M, Mat- Term) causing recurrent venous throm¬
(O) 141 suura Y, Li SS-L, Kanno T: Detection bosis (DV) 196
Le Marec B —» Dorval I and characterization of new genetic mu¬ Mioni F —» Danieli GA
Lemerle J Bonaiti-Pellie C tations in individuals heterozygous for Mitchell DC Millar DS
Leonard A —» Tarlow JK lactate dehydrogenase-B(H) deficiency Mitulla B —> Thieme A
Lenz W, Zygulska M, Horst J: FFU com¬ using DNA conformation polymorphism Miwa S —» Hirono A
plex: an analysis of 491 ca.ses (O) 347 analysis and silver staining (O) 163 Miyazaki H —» Nakahashi Y
Lettau R —» Neuber M Malcolm S —» Jones AM Moerman P —» Fryns JP
Leversha MA —»Tzimagiorgis G Malcolm S Lovering R Moi P —> Perichon B
Levinsky RJ —* Jones AM Malcolm S —» O’Reilly M-AJ Molano J —> Ezquieta B
Levinsky RJ —» Lovering R Malfoy B Almeida A Moore K —* Lebo RV
VII
Moore MR Norton B Oppenheim A, Jury CL, Rund D, Vulliamy Powers PK Hixson JE
Morin D -4 Poulat F TJ, Luzzatto L: G6PD Mediterranean ac¬ Pras E -4 Aksentijevich I
Mortal N —> Casals T counts for the high prevalence of G6PD Pras M —> Aksentijevich I
Morris C. Courtay C. Geurts van Kessel A, deficiency in Kurdish Jews (SC) 293 Premoli-De-Percoco G, Pinto Cistemas J,
Hoeve J ten, Heisterkamp N, Groffen J: O’Reilly M-AJ —» Lovering R Ramirez JL, Galindo I; Focal epithelial
Localization of a gamma-glutamyl-trans- O’Reilly M-AJ, Sweatman AK, Bradley hyperplasia: human-papillomavirus-in-
ferase-related gene family on chromo¬ LD, Alterman LA, Lovering R, Malcolm duced disease with a genetic predisposi¬
some 22 (O) 31 S, Levinsky RJ, Kinnon C: Isolation and tion in a Venezuelan family (SC) 386
Morrison MJ —> Crossen PE mapping of discrete DXSIOI loci in Prockop DJ —» Zhuang J
Morrison N —> Murphy MT Xq22 near the X-linked agammaglobuli- Propping P Faiyaz ul Haque M
Moschonas NK —> Tzimagiorgis G naemia gene locus (SC) 605 Puig JG Bouwens-Rombouts AGM
Moser H Sander A O’Riordan JLH —* Rowe PSN Pujia A —> Marasco O
Mostacciuolo ML —» Danieli GA Osborne LC, Mason JM: HLA-A/B haplo- Punnett HH Lebo RV
Mountford R —» Rowe PSN tye frequencies among U.S. Hispanic
Miiller CR —* Danieli GA and African-American populations (O) Quaresima B —> Marasco O
Muller U, Wachtel SS, Jaswaney VL, 326 Quere I —» Guillermit H
Goldberg EH: H-Y (SDM) antibody Oshima A —> Suzuki Y
specifically binds Mullerian inhibiting Oudet C —> Rowe PSN Raefle G Shipman R
substance (L) 515 Ouweland AMW van den —> Dreesen Raghunath M —¥ Mackay K
Murphy MT, Morrison N, Miles JS, Fraser JCFM Ragnarsson J —» Fossdal R
RH, Spurr NK, Boyd E; Regional chro¬ Ragusa A —> Perichon B
mosomal assignment of the Kell blood Palacio A —> Casals T Rahmani Z Crete N
group locus (KEL) to chromosome Palmer CG —» Planner R Ramasawmy R, Kotea N, Lu C, Sayada C,
7q33-<j35 by fluorescence in situ hy¬ Pankau R —» Traupe H Baligadoo S, Krishnamoorthy R: A new
bridization: evidence for the polypeptide Pargent W Schaible G polymorphic restriction site at the human
nature of antigenic variation (O) 585 Parkinson DB, Shaw NJ, Himsworth RL, atrial natriuretic peptide (hANP) gene
Muscatelli F Lefebvre S Thakker RV: Parathyroid hormone gene locus (DV) 509
analysis in autosomal hypoparathy¬ Ramirez JL —» Premoli-De-Percoco G
Naitoh Y —> Nakahashi Y roidism using an intragenic tetranu- Rappold GA —> Schaible G
Nakahashi Y, Miyazaki H, Kadota Y, cleotide (AAAT)„ polymorphism (SC) Raveh J —> Sander A
Naitoh Y, Inoue K, Yamamoto M, 281 Read A Rowe PSN
Hayashi N, Taketani S: Molecular defect Pelicci P-G Huebner K Redila-Flores MT —> Lebo RV
in human erythropoietic protoporphyria Peltomaki P Larramendy M Rehder H —> Neuber M
with fatal liver failure (O) 303 Pengue G —» Huebner K Reiss J, Ellermeyer U, Schloesser M,
Nakamura M, Fujiwara Y, Yamamoto M: Perichon B, Ragusa A, Lapoumeroulie C, Fuhrmann W, Drews D, Posselt HG:
The two locus control of Leber heredi¬ Romand A, Moi P, Ikuta T, Labie D, Two cystic fibrosis patients with the
tary optic neurophathy and a high pene¬ Elion J, Krishnamoorthy R: Inter-ethnic genotype G542X/G551D (CC) 78
trance in Japanese pedigrees (O) 339 polymorphism of the |i-globin gene lo¬ Reshef A —» Leitersdorf E
Nakamura Y —» Petersen GM cus control region (LCR) in sickle-cell Ritter H —> Krczal D
Nakasono I —> Kubo S anemia patients (O) 464 Ritvanen A —> Larramendy M
Nakayasu K —» Zhuang J Perrotti N —» Marasco O Roberts SH —> Upadhyaya M
Narcisi TME —> Shoulders CC Peters D —» Fossdal R Robinson WP, Spiegel R, Schinzel AA:
Narins SC Wise RJ Petersen GM, Francomano C, Kinzler K, Deletion breakpoints associated with
Neuber M, Rehder H, Zuther C, Lettau R, Nakamura Y: Presymptomatic direct de¬ the Prader-Willi and Angelman syn¬
Schwinger E: Polyploidies in abortion tection of adenomatous polyposis coli dromes (15ql l-ql3) are not sites of high
material decrease with maternal age (APC) gene mutations in familial adeno¬ homologous recombination (O) 181
(O) 563 matous polyposis (O) 307 Rodenhiser DI Ainsworth PJ
Nicoletti B Tedeschi B Peverali G Bardoni B Roechel N —» Giuili G
Niikawa N —> Fukushima Y Pezzolo A —> Ghiggeri GM Romand A —> Perichon B
Nordenskjold M —> Lindblom A Philippon G Martinson JJ Rooij F de —> Gu X-F
Nordmann Y ^ Gu X-F Picciotti E Marasco O Ropers HH Mariman ECM
Norton B, Lanyon WG, Moore MR, Por- Pinto Cistemas J —» Premoli-De-Percoco G Ropers H-H —^ Traupe H
teous M, Youngs GR, Connor JM: Evi¬ Planner R, Heerema NA, Howard-Peebles Ropers H-H —» Vries DD de
dence for involvement of a second ge¬ PN, Miles JH, Soukup S, Palmer CG: Rosso C —> Ghia P
netic locus on chromosome 1 Iq in por¬ Clinical findings in patients with marker Roth M-P Stoll C
phyrin metabolism (O) 576 chromosomes identified by fluorescence Rotstein S —> Lindblom A
Niimberg P, Thiel G, Weber F, Epplen JT; in situ hybridization (O) 589 Roussey M Dorval I
Changes of telomere lengths in human Planner R, Heerema NA, Yurov YB, Roux J —» Martinson JJ
intracranial tumours (SC) 190 Palmer CG: Efficient identification of Rowe PSN, Goulding J, Read A, Mount-
Nunes V —> Casals T marker chromosomes in 27 patients by ford R, Hanauer A, Oudet C, Whyte
stepwise hybridization with alpha-satel¬ MP, Meier-Ewert S, Lehrach H, Davies
Odent S —> Dorval I lite DNA probes (O) 131 KE, O’Riordan JLH: New markers for
Ogata T, Matsuo N: Sex chromosome Poller W —> Liidecke B linkage analysis of X-linked hypophos-
aberrations and stature: deduction of the Porcellini A Marasco O phataemic rickets (O) 571
principal factors involved in the determi¬ Porteous M —» Norton B Rowe RA —> Sawyer JR
nation of adult height (O) 551 Posselt HG —» Reiss J Royer-Pokora B —> Schneider S
Ohashi H —» Fukushima Y Poulat F, Morin D, Konig A, Brun P, Rudiger N —» Klausen IC
Ohno T —> Fukushima Y Giltay J, Sultan C, Dumas R, Gessler M, Rund D —> Oppenheim A
Olek K Liidecke B Berta P: Distinct molecular origins for
Oost BA van —> Dreesen JCFM Denys-Drash and Frasier syndromes Saint-Jore B, Loux N, Junien C, Boileau
Oost BA van —» Vries DD de (SC) 285 C: Two new polymorphisms in the cod-
1
1
VIII
ing sequence of the LDL receptor ing region of the apo AI gene (DV) splice-site mutation in the low density
(LDLR) gene (DV) 511 197 lipoprotein receptor gene by denaturing
Salonen R —» Hyden-Granskog C Shull MM -» Lebo RV gradient gel electrophoresis (O) 480
Sander A. Moser H. Liechti-Gallati S. Sim RB —» Steinkasserer A Toumade M-F —» Bonaiti-Pellie C
Grimm T. Zingg M. Raveh J: Linkage Simola K —» Larramendy M Traupe H, Vetter U, Happle R. Fisher LW,
of Van der Woude syndrome (VV*’S) to Sinet P-M —» Cr6te N Cremers FPM, Landy SJ, Pankau R,
REN and exclusion of the candidate Skoog L —» Lindblom A Ropers H-H: Exclusion of the biglycan
gene TGFB2 from the disease locus in a Smith PJ —* Byrne JA (BGN) gene as a candidate gene for the
large pedigree (O) 55 Smits APT —» Dreesen JCFM Happle syndrome, employing an intra¬
Sanna ML —» Tedeschi B Solari R —* Tarlow JK genic single-strand conformational poly¬
Sano A. Kondoh K. Kakiimno Y. Kondo I; Sommer SS -* Bottema CDK morphism (L) 89
A 40-nucleotide repeat polymorphism in Soukup S —> Plattner R Trofatter J —> Lebo RV
the human dopamine transporter gene Spadoni GL —» Tedeschi B Tromp G —* Zhuang J
(DV) 405 Spiegel R —» Robinson WP Tsai MY, Holzknecht RA, Tuchman M:
Sargent CA —* Tzimagiorgis G Spiegler AWJ —» Thieme A Single-strand conformational polymor¬
Sawyer JR. Rowe RA. Massed SJ. Cunniff Spurr NK —> Murphy MT phism and direct sequencing applied to
C: High-resolution cytogenetic charac¬ SteinbeiBer T —> Assum G carrier testing in families with ornithine
terization of telomeric associations in Steinkasserer A. Ddmer C, Wiirzner R, transcarbamylase deficiency (O) 321
ring chromosome 19 (O) 42 Sim RB: Human (J^-glycoprotein I: mol¬ Tsuda R Kubo S
Sayada C —* Ramasawmy R ecular analysis of DNA and amino acid Tuchman M —> Tsai MY
Sch^hter F. Cohen D. Kirkwood T: polymorphism (DV) 401 Tuck-Muller CM, Martinez JE, Batista
Prospects for the genetics of human Steinkasserer A —» Tarlow JK DAS, Kearns WG, Wertelecki W: Dupli¬
longevity (R) 519 Steinmann B —¥ Mackay K cation of the short arm of the X chromo¬
Schaible G. Rappold GA. Pargent W, Stoll C. Dott B, Alembik Y, Roth M-P: some in mother and daugther (CC) 395
Zachau HG; The immunoglobulin K Evaluation of routine prenatal ultrasound Turpin JC —» Lucotte G
locus: polymorphism and haplotypes examination in detecting fetal chromoso¬ Tzimagiorgis G, Leversha MA, Chroniary
of Caucasoid and rK>n-Caucasoid indi¬ mal abnormalities in a low risk popula¬ K, Goulielmos G, Sargent CA, Fergu-
viduals (O) 261 tion (O) 37 son-Smith M, Moschonas NK: Structure
Scheffer H Kooy RF Sudo K —* Maekawa M and expression analysis of a member of
Schenkein HA —» Hart TC Sultan C —* Poulat F the human glutamate dehydrogenase
Scherthan H —> Seisenberger C Suzuki Y, Oshima A: A P-galactosidase (GLUD) gene family mapfied to chro¬
Schertzer M —* Wood S gene mutation identified in both mosome I Op 11.2 (O) 433
Schinzel AA —» Robinson WP Morquio B disease and infantile G^i
Schloesser M —* Reiss J gangliosidosis (L) 407
Ueoka Y —» Fukushima Y
Schneider S. Wildhardt G, Ludwig R, Sweatman AK —» Lovering R
Uhlhaas S —> Faiyaz ul Haque M
Royer-Pokora B: Exon skipping due to a Sweatman AK —» O’Reilly M-AJ
Umenishi F —> Kajii E
mutation in a donor splice site in the
Upadhyaya M, Roberts SH, Famham J,
WT-I gene is associated with Wilms' Takeda R —* Inazu A
MacMillan JC. Clarke A, Heath JP,
tumor and severe genital malformations Takegoshi T —> Inazu A
Hodges ICG, Harper PS: Charcot-Marie-
(O) 599 Taketani S —» Nakahashi Y
Tooth disease IA (CMTIA) associated
Scholl U ^ Giuili G Tarlow JK. Blakemore AIF, Leonard A,
with a maternal duplication of chromo¬
Schonberg SA —» Lebo RV Solari R, Hughes HN, Steinkasserer A,
some 17p 11.2^12 (SC) 392
SchramI P —* Shipman R Duff GW: Polymorphism in human IL-I
Schuler H —» Faiyaz ul Haque M receptor antagonist gene intron 2 is
Schulze F —»Thieme A caused by variable numbers of an 86-bp Vandenberghe K —* Fryns JP
Schuster H. Fischer HJ. Keller C. Wolfram tandem repeat (DV) 403 Van der Veen AY —> Kooy RF
G. Zollner N: Identirication of the 408 Tartary M —» Vidaud D Veile R Howe JR
valine to methionine mutation in the Tedeschi B, Spadoni GL. Sanna ML, Ver- Verlind E —> Kooy RF
low density lipoprotein receptor in a nole P, Caporossi D, Cianfarani S, Nico- Vemole P —> Tedeschi B
German family with familial hyper¬ letti B, Boscherini B: Increased chromo¬ Vetter U —* Traupe H
cholesterolemia (SC) 287 some fragility in lymphocytes of short Vicario JL —» De Juan D
Schwinger E —♦ Neuber M normal children treated with recombi¬ Vidaud D, Tartary M, Costa J-M, Bahnak
Scott J —» Shoulders CC nant human growth hormone (O) 459 BR, Gispert-Sanchez S, Fressinaud E,
Seisenberger C. Winnacker E-L, Scherthan Te Velde K -» Gu X-F Gazengel C, Meyer D, Goossens M,
H: Localisation of the human nuclear Thakker RV —» Parkinson DB Lavergne J-M, Vidaud M: Nucleotide
factor I/X (NR/X) gene to chromosome Thiel G, Lozanova T, Vogel S, Kintzel D, substitutions at the -6 position in the
I9pl3 and detection of five other related Janisch W, Witkowski R: Age-related promoter region of the factor IX gene re¬
loci at lp2l-22. lq42-43, 5ql5, I Ipl3 nonrandom chromosomal abnormalities sult in different severity of hemophilia B
and20ql3by FISH(O) 535 in human low-grade astrocytomas (O) Leyden: consequences for genetic coun¬
Serra A —» Ghia P 547 seling (O) 241
Shapiro A —* Bottema CDK Thiel G —> Niimberg P Vidaud M Vidaud D
Shaw NJ —» Parkinson DB Thieme A, Mitulla B, Schulze F, Spiegler Viegas-Pequignot E —> Almeida A
Sheffield U ^ Loesch DZ AWJ: Epidemiological data on Werdnig- Vielhaber E —» Bottema CDK
Sheffield VC ^ Beck JS Hoffmann disease in Germany (West- Vigna MF —> Marasco O
Shipman R, SchramI P, Colombi M. Raefle Thiiringen) (SC) 295 Vitiello L Danieli GA
G, Ludwig CU: Loss of heterozygosity Thiesen HJ —» Cannizzaro LA Vizzone A ^ De Vita R
on chromosome 11 pi 3 in primary blad¬ Tilanus MGJ —* Bouwens-Rombouts Vogel S —» Thiel G
der carcinoma (O) 455 AGM Voute PA —» Bonaiti-Pellie C
Shoulders CC, Narcisi TME. Jarmuz A. Tobler A —» Fey MF Vries DD de, Wijs IJ de, G. Wolff,
Brett DJ, Bayliss JD, Scott J: Characteri¬ Top B, Zee A van der, Havekes LM. Hooft Ketelsen U-P, Ropers H-H, (Dost BA
zation of genetic markers in the 5' flank¬ FM van't. Frants RR: Identification of a van: X-linked myoclonus epilepsy ex-
IX
plained as a maternally inherited mito¬ Winnacker E-L —> Seisenberger C Zee A van der —> Top B
chondrial disorder (O) 51 Wise RJ, Ewenstein BM, Gorlin J, Narins Zhuang J, Tromp G, Kuivaniemi H,
Vulliamy TJ Oppenheim A SC, Jesson M, Handin RI: Autosomal re¬ Nakayasu K, Prockop DJ: Deletion of 19
cessive transmission of hemophilia A base pairs in intron 13 of the gene for
Wachtel SS ^ Muller U due to a von Willebrand factor mutation the proa2(l) chain of type-I procollagen
Wakasugi T —> Inazu A (O) 367 (COL IA2) causes exon skipping in a
Wakui K Fukushima Y Wissman PB —> Grody WW proband with type-I osteogenesis imper¬
Warren AC, Mclnnis MG. Kalaitsidaki M, Wit E de ^ Knijff P de fecta (O) 210
Cox TK, Blaschak J, Chakravarti A, An- Witkowski R —> Thiel G Zimmer N, Gotten E, Kraus J, Zang KD,
tonarakis SE: D2IS210: A highly poly¬ Wolff G Vries DD de Henn W: Immunophenotyping of mitotic
morphic (GT)n marker closely linked to Wolfram G —* Schuster H cells from long-term cultures of chori¬
the P-amyloid protein precursor (APP) Wood S, Schertzer M. Hayden M, Ma Y: onic villi (O) 317
gene (DV) 87 Support for founder effect for two Zingg M Sander A
Weber F —^ Niimberg P lipoprotein lipase (LPL) gene mutations Zingone A Marasco O
Wedell A, Luthman H: Steroid 21-hydrox¬ in French Canadians by analysis of GT Zdllner N Schuster H
ylase (P450c2l): a new allele and spread microsatellites flanking the LPL gene Zuffardi O —» Bardoni B
of mutations through the pseudogene (O) (O) 312 Zuffardi O —> Ghiggeri GM
236 Woods P ^ Millar DS Zuther C —> Neuber M
Wells SA Jr Howe JR Wiirzner R —> Steinkasserer A Zygulska M Lenz W
Wertelecki W Tuck-Muller CM
Wessman M —> Larramendy M Yagi K —» Inazu A
Westhuyzen DR van der —> Leitersdorf E Yamamoto M —» Nakahashi Y Announcements 302,408,618
Whyte MP -4 Rowe PSN Yamamoto M —> Nakamura M
Wiegant J —> Lebo RV Yaspo M-L Crete N Erratum 301
Wijs IJ de —¥ Vries DD de Yoon H-S —> Bottema CDK
Wildhardt G Schneider S Youngs GR —> Norton B
Wilkinson TA, Crolla JA: Molecular cyto¬ Yurov YB —> Plattner R
genetic characterization of three familial
cases of satellited Y chromosomes (SC) Zachau HG Schaible G
389 Zang KD —» Zimmer N Indexed in Current Contents